HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968810Generated: November 1, 2026
(S)-2-aminopropanamide hydrochloride → HCID 9850447, compound
https://huagongshe.com/reaction/968810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (S)-2-aminopropanamide hydrochloride | HCID 2775816 | — |
| Reactant | HCID 12136446 | HCID 12136446 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 9850447 | HCID 9850447 | 79.6% |
Reaction Steps
L-Alaninamide hydrochloride (0.151 g, 1.209 mmol) was dissolved in anhydrous DMF and DMAP (0.197 g, 1.612 mmol) was added to the solution. The reaction mixture was stirred at room temperature for 1 h. Then, (R)-5-(4-cyano-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-α]imidazole-3-sulfonyl chloride (0.24 g, 0.484 mmol) in anhydrous DMF was added to the reaction mixture and stirred for additional 10 min. The reaction solution was diluted with EtOAc and washed with water, 1 N HCl and then water. The organic phase was dried over Na2SO4 and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford 0.211 g of the title compound as a white scaly solid (M+1, 547.2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304067B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-1d0d7ec743b2410da988546204e3b89e |
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| Source note | uspto-grants-2007_12 |
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